医学
耐火材料(行星科学)
托珠单抗
淋巴瘤
B细胞淋巴瘤
肿瘤科
内科学
材料科学
疾病
复合材料
作者
Frederick L. Locke,Sattva S. Neelapu,Nancy L. Bartlett,Lazaros J. Lekakis,Caron A. Jacobson,Ira Braunschweig,Olalekan O. Oluwole,Tanya Siddiqi,Yi Lin,John M. Timmerman,Marie José Kersten,Yan Zheng,Teresa Zhang,Jenny Nater,Rhine R. Shen,Harry Miao,Jenny Kim,David B. Miklos
标识
DOI:10.1016/j.jtct.2024.08.018
摘要
Axicabtagene ciloleucel (axi-cel) is an autologous anti-CD19 chimeric antigen receptor (CAR) T-cell therapy approved in patients with relapsed/refractory (R/R) large B-cell lymphoma (LBCL). Most patients treated with axi-cel experience cytokine release syndrome (CRS) and/or adverse neurologic events (NEs). To explore potential approaches for reducing CAR T-cell-related toxicities with axi-cel, several safety expansion cohorts were added to the pivotal ZUMA-1 trial. ZUMA-1 Cohort 3 was an exploratory safety cohort that investigated the use of the IL-6 receptor blocking antibody tocilizumab and anticonvulsant levetiracetam as prophylaxis against CRS and NEs in patients treated with axi-cel. Patients with R/R LBCL were enrolled in Cohort 3 and received conditioning chemotherapy on d- 5 through -3 followed by a single infusion of axi-cel (2 × 10
科研通智能强力驱动
Strongly Powered by AbleSci AI